نتایج جستجو برای: hemiplegic migraine
تعداد نتایج: 14930 فیلتر نتایج به سال:
Familial hemiplegic migraine (FHM)-causing mutations in the gene encoding the P/Q Ca(2+) channel alpha(1A) subunit (CACNA1A) locate to the pore and voltage sensor regions and normally involve gain-of-channel function. We now report on a mutation identified in the first intracellular loop of CACNA1A (alpha(1A(A454T))) that does not cause FHM but is associated with the absence of sensorimotor sym...
THE CLINICAL SYNDROME of migraine is estimated to affect 23 to 29% of women and 15 to 20% of men.' This very common condition is characterized by recurrent attacks of headache associated with photophobia, anorexia, nausea, vomiting, and other autonomic disturbances and frequently by striking focal neurological manifestations. The episodes are distinctly varied in frequency, severity, and durati...
Familial hemiplegic migraine type 2 is a premonitory subtype of caused by an ATP1A2 gene mutation. It autosomal dominant genetic disease. Here, we report 51-year-old woman who had attack due to pathogenic With frequent attacks, the patient developed complete left hemiplegia, confusion consciousness and partial seizures. Magnetic resonance imaging showed extensive angiogenic edema in right cereb...
Migraine is a recurrent neurovascular disease. Its two most common forms-migraine without aura (MO) and migraine with aura (MA)-both show familial clustering and a complex pattern of inheritance. Familial hemiplegic migraine (FHM) is a rare monogenic subform caused by mutations in the calcium channel gene CACNA1A or the Na(+)/K(+)-ATPase gene ATP1A2. An involvement of FHM genes in the pathogene...
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